Canonical Allele Identifier: CA448101381

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180036971A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609971A>T , CM000667.2:g.180609971A>T	GRCh38
NC_000005.9:g.180036971A>T , CM000667.1:g.180036971A>T	GRCh37
NC_000005.8:g.179969577A>T	NCBI36
NG_011536.1:g.44654T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3741T>A MANE Select	ENSP00000261937.6:p.Arg1247=
ENST00000261937.10:c.3741T>A	ENSP00000261937.6:p.Arg1247=
ENST00000393347.7:c.3741T>A	ENSP00000377016.3:p.Arg1247=
ENST00000502603.5:n.441T>A
ENST00000502649.5:c.3741T>A	ENSP00000426057.1:p.Arg1247=
ENST00000507059.5:n.4091T>A
ENST00000619105.4:c.*2684T>A	ENSP00000481134.1:n.*2684T>A
NM_002020.4:c.3741T>A	NP_002011.2:p.Arg1247=
NM_182925.4:c.3741T>A	NP_891555.2:p.Arg1247=
XM_011534477.1:c.3990T>A	XP_011532779.1:p.Arg1330=
XM_011534478.1:c.3972T>A	XP_011532780.1:p.Arg1324=
XM_011534479.1:c.3990T>A	XP_011532781.1:p.Arg1330=
XM_011534480.1:c.3990T>A	XP_011532782.1:p.Arg1330=
XM_011534481.1:c.3990T>A	XP_011532783.1:p.Arg1330=
XM_011534482.1:c.3759T>A	XP_011532784.1:p.Arg1253=
XM_011534483.1:c.3681T>A	XP_011532785.1:p.Arg1227=
XM_011534484.1:c.3282T>A	XP_011532786.1:p.Arg1094=
XR_941095.1:n.4027T>A
NM_001354989.1:c.3741T>A	NP_001341918.1:p.Arg1247=
XM_011534478.3:c.3972T>A	XP_011532780.1:p.Arg1324=
XM_011534484.2:c.3282T>A	XP_011532786.1:p.Arg1094=
XM_017009263.1:c.3972T>A	XP_016864752.1:p.Arg1324=
XM_017009264.2:c.3972T>A	XP_016864753.1:p.Arg1324=
XM_017009265.1:c.3972T>A	XP_016864754.1:p.Arg1324=
XM_017009266.1:c.3972T>A	XP_016864755.1:p.Arg1324=
XM_017009267.2:c.3972T>A	XP_016864756.1:p.Arg1324=
XM_017009268.1:c.3663T>A	XP_016864757.1:p.Arg1221=
XR_001742050.2:n.4231T>A
NM_182925.5:c.3741T>A MANE Select	NP_891555.2:p.Arg1247=
NM_001354989.2:c.3741T>A	NP_001341918.1:p.Arg1247=
NM_002020.5:c.3741T>A	NP_002011.2:p.Arg1247=